Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
  • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
  • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
  • C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
  • C07D211/14—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/35—Ketones, e.g. benzophenone
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/41—Amines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
  • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C255/00—Carboxylic acid nitriles
  • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
  • C07C255/30—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same unsaturated acyclic carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/78—Separation; Purification; Stabilisation; Use of additives
  • C07C45/86—Use of additives, e.g. for stabilisation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
  • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
  • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D211/40—Oxygen atoms
  • C07D211/44—Oxygen atoms attached in position 4
  • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
  • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
  • A61K2800/52—Stabilizers
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
  • C07C2601/14—The ring being saturated

Definitions

• the present invention relates to a cosmetic composition
• a cosmetic composition comprising the combination i) of at least one screening agent of the dibenzoylmethane derivative type and ii) of at least one specific merocyanine dicyano or cyanoacetate derivative, the definition of which will be given below.
• It also relates to a method for the photostabilization, with regard to radiation, of at least one screening agent of the dibenzoylmethane derivative type by an effective amount of at least one specific merocyanine dicyano or cyanoacetate derivative, the definition of which will be given below.
• UV-A rays with wavelengths of between 320 and 400 nm, which cause browning of the skin, are capable of bringing about a detrimental change in the latter, in particular in the case of sensitive skin or of skin continually exposed to solar radiation.
• UV-A rays cause in particular a loss in the elasticity of the skin and the appearance of wrinkles, resulting in premature skin ageing. They promote the triggering of the erythemal reaction or accentuate this reaction in some subjects and can even be the cause of phototoxic or photoallergic reactions.
• UV-A rays For aesthetic and cosmetic reasons, such as the preservation of the natural elasticity of the skin, for example, increasingly people desire to control the effect of UV-A rays on their skin. It is therefore desirable also to screen out UV-A radiation.
• antisun compositions comprising organic screening agents which are active in the UV-A region and which are active in the UV-B region.
• the majority of these screening agents are fat- soluble.
• UV-A screening agents are currently composed of dibenzoylmethane derivatives and in particular 4-(tert- butyl)-4'-methoxydibenzoylmethane, this being because these exhibit a high intrinsic absorption power.
• dibenzoylmethane derivatives which are now products well known per se as screening agents active in the UV-A region, are described in particular in French Patent Applications FR-A-2326405 and FR-A-2440933, and in European Patent Application EP-A-01 14607; furthermore, 4-(tert-butyl)-4'-methoxydibenzoylmethane is currently provided for sale under the trade name of "Parsol 1789 ®" by DSM Nutritional Products.
• dibenzoylmethane derivatives are products which are relatively sensitive to ultraviolet radiation (in particular UV-A radiation), that is to say, more specifically, that they exhibit an unfortunate tendency to decompose more or less rapidly under the action of the latter.
• UV-A radiation ultraviolet radiation
• this substantial lack of photochemical stability of dibenzoylmethane derivatives in the face of the ultraviolet radiation to which they are by nature intended to be subjected does not make it possible to guarantee continuous protection during prolonged exposure to the sun, so that repeated applications at regular and close intervals of time have to be carried out by the user in order to obtain effective protection of the skin against UV rays.
• Patent Application WO 0128732 reveals a method for the photostabilization of a dibenzoylmethane derivative by a merocyanine phenyl sulphone derivative.
• this photostabilization of the dibenzoylmethane derivative by the merocyanine phenyl sulphone derivative is not completely satisfactory.
• these merocyanine phenyl sulphone derivatives exhibit the disadvantage of decomposing in the presence of dibenzoylmethane under the influence of UV radiation.
• the Applicant Company has now just discovered, surprisingly, that, by combining the abovementioned dibenzoylmethane derivatives with at least one specific merocyanine dicyano or cyanoacetate derivative, the definition of which will be given below, it is possible to substantially further improve the photochemical stability (or photostability) of these same dibenzoylmethane derivatives and their effectiveness in the UV-A region without the disadvantages indicated above.
• composition comprising, in a cosmetically acceptable vehicle, at least one UV screening system, characterized in that it comprises:
• At least one merocyanine dicyano or cyanoacetate derivative (ii) at least one merocyanine dicyano or cyanoacetate derivative, the definitions of which will be given below.
• Another subject-matter of the invention is also a method for improving the chemical stability with regard to UV radiation of at least one dibenzoylmethane derivative which consists in combining the said dibenzoylmethane derivative with an effective amount of at least one merocyanine dicyano or cyanoacetate derivative, the definitions of which will be given below.
• Cosmetically acceptable is understood to mean compatible with the skin and/or its superficial body growths, exhibiting a pleasant colour, a pleasant odour and a pleasant feel, and not causing unacceptable discomfort (smarting, tightness, redness) liable to dissuade the consumer from using this composition.
• Effective amount is understood to mean an amount sufficient to produce a notable and significant improvement in the photostability of the dibenzoylmethane derivative or derivatives in the cosmetic composition.
• This minimum amount of merocyanine dicyano or cyanoacetate derivative as described in detail later, which can vary according to the nature of the vehicle selected for the composition, can be determined without any difficulty by means of a conventional test for measuring photostability, such as that given in the examples below.
• the dibenzoylmethane derivative or derivatives can be present in the compositions in accordance with the invention at contents which preferably vary from 0.01 to 20% by weight, more preferably from 0.1 to 10% by weight and more preferably still from 0.1 to 6% by weight, with respect to the total weight of the composition.
• merocyanine dicyano or cyanoacetate derivatives in accordance with the present invention are chosen from the group consisting of:
• Ri and R2 which are identical or different, denote a linear or branched C1-C3 alkyl radical, the hydroxyethyl group or a C5-C6 cycloalkyl,
• R3 denotes a linear or branched Ci-Cs alkyl radical
• Ri , R 2 or R 3 is a C2-C16 alkyl diradical or else Ri and R2 form, with 2 nitrogen atoms, a cyclic divalent -(CH 2 ) m - radical with m being an integer ranging from 3 to 7;
• the compounds of formula (I) and the compounds (a), (b), (c), (I), (p), (v), (w), (x), (aa) and (bb) can be in the ⁇ , ⁇ -, ⁇ , ⁇ - or ⁇ , ⁇ - geometrical isomeric forms.
• n 2
• diradical is understood to mean a divalent radical so that the two units are bonded to one another via this diradical. Mention may be made, by way of illustration, of the following compounds q and r:
• Ci-Cs alkyl radicals for example, of methyl, ethyl, n-propyl, 1 -methylethyl, isopropyl, n-butyl, 1 -methyl propyl, 2- methyl propyl, 1 ,1 -dimethylethyl, n-pentyl, 1 -methylbutyl, 2-methyl butyl, 3- methylbutyl, 2,2-dimethylpropyl, 1 -ethylpropyl, n-hexyl, 1 ,1 -dimethylpropyl, 1 ,2- di methyl propyl, 1 -methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1 ,1 -dimethylbutyl, 1 ,2-dimethylbutyl, 1 ,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3- dimethylbut
• R 3 and n have the same meanings as in the formula (I), and their ⁇ , ⁇ -, ⁇ , ⁇ - or ⁇ , ⁇ - isomeric forms.
• the hydrophilic or water-soluble merocyanine screening agent or agents in accordance with the invention can be present in the compositions according to the invention at a concentration of between 0.1 and 10% by weight, preferably between 0.2 and 5% by weight, with respect to the total weight of the composition.
• compositions in accordance with the invention can additionally comprise other additional organic or inorganic UV screening agents which are active in the UV-A and/or UV-B regions and which are water-soluble or fat-soluble or else insoluble in the cosmetic solvents commonly used.
• the additional organic screening agents are chosen in particular from anthranilics; cinnamic derivatives; salicylic derivatives; benzylidenecamphor derivatives; benzophenone derivatives; ⁇ , ⁇ -diphenylacrylate derivatives; triazine derivatives; phenylbenzotriazole derivatives; benzalmalonate derivatives, in particular those cited in Patent US 5 624 663; phenylbenzimidazole derivatives; imidazolines; bis-benzazolyl derivatives, such as described in Patents EP 669 323 and US 2 463 264; p-aminobenzoic acid (PABA) derivatives; methylenebis(hydroxyphenylbenzotriazole) derivatives, such as described in Applications US 5 237 071 , US 5 166 355, GB 2 303 549, DE 197 26 184 and EP 893 1 19; benzoxazole derivatives, such as described in Patent Applications EP 0 832 642, EP 1 027 883,
• Ethylhexyl Dimethyl PABA sold in particular under the name "Escalol 507" by ISP,
• PEG-25 PABA sold under the name "Uvinul P25" by BASF,
• Ethylhexyl Methoxycinnamate sold in particular under the trade name "Parsol MCX” by DSM Nutritional Products,
• Octocrylene sold in particular under the trade name "Uvinul N539” by BASF
• Etocrylene sold in particular under the trade name "Uvinul N35” by BASF
• Benzophenone-1 sold under the trade name "Uvinul 400" by BASF,
• Benzophenone-2 sold under the trade name "Uvinul D50" by BASF,
• Benzophenone-3 or Oxybenzone sold under the trade name "Uvinul M40" by BASF,
• Benzophenone-4 sold under the trade name "Uvinul MS40" by BASF,
• Benzophenone-6 sold under the trade name "Helisorb 1 1 " by Norquay,
• Benzophenone-8 sold under the trade name "Spectra-Sorb UV-24" by American Cyanamid,
• Benzophenone-9 sold under the trade name "Uvinul DS-49" by BASF,
• n-Hexyl 2-(4-diethylamino-2-hydroxybenzoyl)benzoate sold under the trade name "Uvinul A +" or in the form of a mixture with octyl methoxycinnamate under the trade name "Uvinul A + B" by BASF,
• Camphor Benzalkonium Methosulfate manufactured under the name "Mexoryl SO" by Chimex,
• Phenylbenzimidazole Sulfonic Acid sold in particular under the trade name “Eusolex 232" by Merck, Disodium Phenyl Dibenzimidazole Tetrasulfonate, sold under the trade name "Neo Heliopan AP” by Symrise,
• Drometrizole Trisiloxane sold under the name "Silatrizole” by Rhodia Chimie
• Methylene Bis-Benzotriazolyl Tetramethylbutylphenol sold in the solid form under the trade name "Mixxim BB/100” by Fairmount Chemical or in the micronized form in aqueous dispersion under the trade name "Tinosorb M” by Ciba Specialty Chemicals,
• Ethylhexyl Triazone sold in particular under the trade name "Uvinul T150" by BASF,
• Polyorganosiloxane comprising benzalmalonate functional groups such as Polysilicone-15, sold under the trade name "Parsol SLX” by Hoffmann-LaRoche,
• the preferred additional organic screening agents are chosen from:
• the additional inorganic screening agents are chosen from coated or uncoated metal oxide pigments, such as, for example, pigments formed of titanium oxide (amorphous or crystalline in the rutile and/or anatase form), iron oxide, zinc oxide, zirconium oxide or cerium oxide, which are all UV photoprotective agents well known per se.
• coated or uncoated metal oxide pigments such as, for example, pigments formed of titanium oxide (amorphous or crystalline in the rutile and/or anatase form), iron oxide, zinc oxide, zirconium oxide or cerium oxide, which are all UV photoprotective agents well known per se.
• the pigments may or may not be coated.
• the coated pigments are pigments which have been subjected to one or more surface treatments of chemical, electronic, mechanochemical and/or mechanical nature with compounds such as described, for example, in Cosmetics & Toiletries, February 1990, Vol. 105, pp. 53-64, such as amino acids, beeswax, fatty acids, fatty alcohols, anionic surfactants, lecithins, sodium, potassium, zinc, iron or aluminium salts of fatty acids, metal alkoxides (titanium or aluminium alkoxides), polyethylene, silicones, proteins (collagen, elastin), alkanolamines, silicon oxides, metal oxides or sodium hexametaphosphate.
• the silicones are organosilicon polymers or oligomers comprising a linear or cyclic and branched or crosslinked structure, of variable molecular weight, obtained by polymerization and/or polycondensation of suitably functionalized silanes and essentially composed of a repetition of main units in which the silicon atoms are connected to one another via oxygen atoms (siloxane bond), optionally substituted hydrocarbon radicals being connected directly to the said silicon atoms via a carbon atom.
• silicones also encompasses the silanes necessary for their preparation, in particular alkylsilanes.
• the silicones used for the coating of the pigments suitable for the present invention are preferably chosen from the group consisting of alkylsilanes, polydialkylsiloxanes and polyalkylhydrosiloxanes. More preferably still, the silicones are chosen from the group consisting of octyltrimethylsilane, polydimethylsiloxanes and polymethylhydrosiloxanes.
• the pigments formed of metal oxides may, before their treatment with silicones, have been treated with other surfacing agents, in particular with cerium oxide, alumina, silica, aluminium compounds, silicon compounds or their mixtures.
• coated pigments are, for example, titanium oxides coated:
• titanium oxide pigments treated with a silicone are, for example, T1O2 treated with octyltrimethylsilane, such as that sold under the trade name "T 805" by Degussa Silices, T1O2 treated with a polydimethylsiloxane, such as that sold under the trade name "70250 Cardre UF TiO2SI3" by Cardre, or anatase/rutile T1O2 treated with a polydimethylhydrosiloxane, such as that sold under the trade name "Microtitanium Dioxide USP Grade Hydrophobic" by Color Techniques.
• T1O2 treated with octyltrimethylsilane such as that sold under the trade name "T 805" by Degussa Silices
• T1O2 treated with a polydimethylsiloxane such as that sold under the trade name "70250 Cardre UF TiO2SI3" by Cardre
• the uncoated titanium oxide pigments are, for example, sold by Tayca under the trade names "Microtitanium Dioxide MT 500 B” or “Microtitanium Dioxide MT600 B", by Degussa under the name “P 25”, by Wacker under the name “Oxyde de titane transparent PW”, by Miyoshi Kasei under the name “UFTR”, by Tomen under the name “ITS” and by Tioxide under the name "Tioveil AQ”.
• the uncoated zinc oxide pigments are, for example:
• Nanophase Technologies those sold under the name “Nanogard WCD 2025” by Nanophase Technologies.
• coated zinc oxide pigments are, for example:
• Nanophase Technologies sold under the name “Nanogard Zinc Oxide FN” by Nanophase Technologies (as a 40% dispersion in Finsolv TN, C12-C15 alkyl benzoate);
• the uncoated cerium oxide pigments are sold, for example, under the name "Colloidal Cerium Oxide” by Rhone-Poulenc.
• the uncoated iron oxide pigments are, for example, sold by Arnaud under the names "Nanogard WCD 2002 (FE 45B)", “Nanogard Iron FE 45 BL AQ”, “Nanogard FE 45R AQ” or “Nanogard WCD 2006 (FE 45R)", or by Mitsubishi under the name "TY-220".
• the coated iron oxide pigments are, for example, sold by Arnaud under the names "Nanogard WCD 2008 (FE 45B FN)", “Nanogard WCD 2009 (FE 45B 556)", “Nanogard FE 45 BL 345" or “Nanogard FE 45 BL”, or by BASF under the name "Oxyde de fer transparent”.
• the additional UV screening agents are generally present in the compositions according to the invention in proportions ranging from 0.01 to 20% by weight, with respect to the total weight of the composition, and preferably ranging from 0.1 to 10% by weight, with respect to the total weight of the composition.
• compositions in accordance with the present invention can additionally comprise conventional cosmetic adjuvants chosen in particular from oils, waxes, organic solvents, ionic or nonionic and hydrophilic or lipophilic thickeners, softening agents, humectants, opacifiers, stabilizing agents, emollients, silicones, antifoaming agents, fragrances, preservatives, anionic, cationic, nonionic, zwitterionic or amphoteric surfactants, active principles, fillers, polymers, propellants, basifying or acidifying agents or any other ingredient commonly used in the cosmetics and/or dermatological field.
• conventional cosmetic adjuvants chosen in particular from oils, waxes, organic solvents, ionic or nonionic and hydrophilic or lipophilic thickeners, softening agents, humectants, opacifiers, stabilizing agents, emollients, silicones, antifoaming agents, fragrances, preservatives, anionic, cationic,
• oils for example, of mineral oils (liquid paraffin); vegetable oils (sweet almond, macadamia, blackcurrant seed or jojoba oil); synthetic oils, such as perhydrosqualene, fatty alcohols, fatty amides (such as isopropyl lauroyl sarcosinate, sold under the name of "Eldew SL-205" by Ajinomoto), fatty acids or esters, such as C12-C15 alkyl benzoate, sold under the trade name "Finsolv TN” or “Witconol TN” by Witco, 2-ethylphenyl benzoate, such as the commercial product sold under the name X-Tend 226 ® by ISP, octyl palmitate, isopropyl lanolate, triglycerides, including those of capric/caprylic acids, dicaprylyl carbonate, sold under the name "Cetiol CC" by Cognis, or oxye
• wax for example, of carnauba wax, beeswax, hydrogenated castor oil, polyethylene waxes and polymethylene waxes, such as that sold under the name Cirebelle 303 by Sasol.
• organic solvents for example, of lower alcohols and polyols.
• the latter can be chosen from glycols and glycol ethers, such as ethylene glycol, propylene glycol, butylene glycol, dipropylene glycol or diethylene glycol.
• hydrophilic thickeners for example, of carboxyvinyl polymers, such as the Carbopols (Carbomers) and the Pemulens (acrylate/Cio-C3o alkyl acrylate copolymer); polyacrylamides, such as, for example, the crosslinked copolymers sold under the names Sepigel 305 (CTFA name: polyacrylamide/C13-14 isoparaffin/Laureth 7) or Simulgel 600 (CTFA name: acrylamide/sodium acryloyldimethyltaurate copolymer/ isohexadecane/polysorbate 80) by Seppic; optionally crosslinked and/or neutralized polymers and copolymers of 2-acrylamido-2- methylpropanesulphonic acid, such as the poly(2-acrylamido-2- methylpropanesulphonic acid) sold by Hoechst under the trade name "Hostacerin AMPS" (CTFA name: ammonium polyacryloyld
• lipophilic thickeners for example, of synthetic polymers, such as the poly(Cio-C3o alkyl acrylates) sold under the names "Intelimer IPA 13-1 " and "Intelimer IPA 13-6" by Landec, or of modified clays, such as hectorite and its derivatives, such as the products sold under the Bentone names.
• compositions according to the invention can be prepared according to techniques well known to a person skilled in the art. They can be provided in particular in the form of a simple or complex (O/W, W/O, O/W/O or W/O/W) emulsion, such as a cream, a milk or a cream gel; in the form of an aqueous gel; or in the form of a lotion.
• a simple or complex (O/W, W/O, O/W/O or W/O/W) emulsion such as a cream, a milk or a cream gel; in the form of an aqueous gel; or in the form of a lotion.
• compositions according to the invention can optionally be packaged as an aerosol and be provided in the foam or spray form.
• the compositions according to the invention are provided in the form of an oil-in-water or water-in-oil emulsion.
• the emulsification processes which can be used are of the paddle or propeller, rotor-stator and HPH type.
• HPH between 50 and 800 bar
• the emulsions generally comprise at least one emulsifying surfactant chosen from amphoteric, anionic, cationic or nonionic emulsifying surfactants, used alone or as a mixture.
• the emulsifiers are appropriately chosen according to the emulsion to be obtained (W/O or O/W emulsion).
• emulsifying surfactants which can be used for the preparation of the W/O emulsions, for example, of alkyl esters or ethers of sorbitan, of glycerol or of sugars; or silicone surfactants, such as dimethicone copolyols, for example the mixture of cyclomethicone and of dimethicone copolyol sold under the name "DC 5225 C” by Dow Corning, and alkyl dimethicone copolyols, such as lauryl methicone copolyol, sold under the name "Dow Corning 5200 Formulation Aid” by Dow Corning, or cetyl dimethicone copolyol, such as the product sold under the name Abil EM 90R by Goldschmidt and the mixture of cetyl dimethicone copolyol, of polyglycerol (4 mol) isostearate and of hexyl laurate sold under the name Abil WE
• polyol alkyl esters of polyethylene glycol esters, such as PEG-30 dipolyhydroxystearate, such as the product sold under the name Arlacel P135 by ICI.
• glycerol and/or sorbitan esters for example, of polyglycerol isostearate, such as the product sold under the name Isolan Gl 34 by Goldschmidt; sorbitan isostearate, such as the product sold under the name Arlacel 987 by ICI; sorbitan glyceryl isostearate, such as the product sold under the name Arlacel 986 by ICI, and their mixtures.
• polyglycerol isostearate such as the product sold under the name Isolan Gl 34 by Goldschmidt
• sorbitan isostearate such as the product sold under the name Arlacel 987 by ICI
• sorbitan glyceryl isostearate such as the product sold under the name Arlacel 986 by ICI
• O/W emulsions for example, as emulsifying surfactants, of nonionic emulsifiers, such as oxyalkylenated (more particularly polyoxyethylenated) esters of fatty acids and of glycerol; oxyalkylenated esters of fatty acids and of sorbitan; oxyalkylenated (oxyethylenated and/or oxypropylenated) esters of fatty acids, such as the PEG-100 stearate/glyceryl stearate mixture sold, for example, by ICI under the name Arlacel 165; oxyalkylenated (oxyethylenated and/or oxypropylenated) ethers of fatty alcohols; esters of sugars, such as sucrose stearate; or ethers of fatty alcohol and of sugar, in particular alkyl polyglucosides (APGs), such as decyl glucoside and
• APGs alkyl
• the mixture of the alkyl polyglucoside as defined above with the corresponding fatty alcohol can be in the form of a self-emulsifying composition, for example as described in the document WO-A-92/06778.
• the aqueous phase of the latter can comprise a nonionic vesicular dispersion prepared according to known processes (Bangham, Standish and Watkins, J. Mol. Biol., 13, 238 (1965), FR 2 315 991 and FR 2 416 008).
• compositions according to the invention have applications in a large number of treatments, in particular cosmetic treatments, of the skin, lips and hair, including the scalp, in particular for protecting and/or caring for the skin, lips and/or hair and/or for making up the skin and/or lips.
• Another subject-matter of the present invention is composed of the use of the compositions according to the invention as defined above in the manufacture of products for the cosmetic treatment of the skin, lips, nails, hair, eyelashes, eyebrows and/or scalp, in particular of care products, sun protection products and make-up products.
• the cosmetic compositions according to the invention can, for example, be used as make-up product.
• the cosmetic compositions according to the invention can, for example, be used as care product and/or sun protection product for the face and/or body with a liquid to semi-liquid consistency, such as milks, relatively smooth creams, cream gels or pastes. They can optionally be packaged as an aerosol and be provided in the form of a foam or of a spray.
• compositions according to the invention in the form of vaporizable fluid lotions in accordance with the invention are applied to the skin or hair in the form of fine particles by means of pressurizing devices.
• the devices in accordance with the invention are well known to a person skilled in the art and comprise nonaerosol pumps or "atomizers", aerosol containers comprising a propellant and aerosol pumps using compressed air as propellant. The latter are described in Patents US 4 077 441 and US 4 850 517 (forming an integral part of the content of the description).
• compositions packaged as an aerosol in accordance with the invention generally comprise conventional propellants, such as, for example, hydrofluorinated compounds, dichlorodifluoromethane, difluoroethane, dimethyl ether, isobutane, n-butane, propane or trichlorofluoromethane. They are preferably present in amounts ranging from 15 to 50% by weight, with respect to the total weight of the composition.
• propellants such as, for example, hydrofluorinated compounds, dichlorodifluoromethane, difluoroethane, dimethyl ether, isobutane, n-butane, propane or trichlorofluoromethane. They are preferably present in amounts ranging from 15 to 50% by weight, with respect to the total weight of the composition.
• the compositions according to the invention can, in addition, also comprise additional cosmetic and determatological active principles.
• - moisturizing agents such as, for example, polyols, such as glycerol, butylene glycol or propylene glycol;
• composition can comprise at least one ingredient, such as fillers having a soft focus effect or agents which promote the natural colouring of the skin, intended to supplement the biological effect of these active principles or to contribute an immediate visual antiaging effect.
• ingredient such as fillers having a soft focus effect or agents which promote the natural colouring of the skin, intended to supplement the biological effect of these active principles or to contribute an immediate visual antiaging effect.
• composition can comprise at least one additional ingredient intended to contribute an immediate visual effect. Mention may in particular be made of agents which promote the naturally pink colouring of the skin.
• agents which promote the naturally pink colouring of the skin for example, of self-tanning agents, that is to say an agent which, applied to the skin, in particular to the face, makes it possible to obtain a tanning effect with an appearance more or less similar to that which can result from prolonged exposure to the sun (natural tanning) or under a UV lamp.
• DHA dihydroxyacetone
• the self-tanning agents are generally chosen from mono- or polycarbonyl compounds, such as, for example, isatin, alloxan, ninhydrin, glyceraldehyde, mesotartaric aldehyde, glutaraldehyde, erythrulose, pyrazoline-4,5-dione derivatives, such as described in Patent Applications FR 2 466 492 and WO 97/35842, dihydroxyacetone (DHA) or 4,4-dihydroxypyrazolin-5-one derivatives, such as described in Patent Application EP 903 342. Use will preferably be made of DHA.
• the DHA can be used in the free and/or encapsulated form, for example encapsulated in lipid vesicules, such as liposomes, described in particular in Application WO 97/25970.
• the self-tanning agent is present in an amount ranging from 0.01 to 20% by weight and preferably in an amount of between 0.1 and 10% of the total weight of the composition.
• Use may also be made of other dyes which make it possible to modify the colour produced by the self-tanning agent.
• These dyes can be chosen from synthetic or natural direct dyes.
• dyes can be chosen, for example, from red or orange dyes of the fluoran type, such as those described in Patent Application FR 2 840 806. Mention may be made, for example, of the following dyes:
• CTFA name CI 45380 or Red 21 ;
• dyes can also be chosen from anthraquinones, caramel, carmine, carbon black, azulene blues, methoxsalen, trioxsalen, guaiazulene, chamazulene, rose bengal, eosin 10B, cyanosine or daphinine.
• dyes can also be chosen from indole derivatives, such as monohydroxy- indoles, such as described in Patent FR 2 651 126 (i.e.: 4-, 5-, 6- or 7- hydroxyindole), or dihydroxyindoles, such as described in Patent EP-B-0 425 324 (i.e.: 5,6-dihydroxyindole, 2-methyl-5,6-dihydroxyindole, 3- methyl-5,6-dihydroxyindole or 2,3-dimethyl-5,6-dihydroxyindole).
• indole derivatives such as monohydroxy- indoles, such as described in Patent FR 2 651 126 (i.e.: 4-, 5-, 6- or 7- hydroxyindole), or dihydroxyindoles, such as described in Patent EP-B-0 425 324 (i.e.: 5,6-dihydroxyindole, 2-methyl-5,6-dihydroxyindole, 3- methyl-5,6-
• 3-Anilinoacrolein-aniline (3 g, 13.5 x 10 "3 mol) and n-butyl cyanoacetate (1 .9 ml, 13.5 x 10 "3 mol) are heated in 6 ml of acetic anhydride for 1 hour 30 minutes at 85-90°C while bubbling with nitrogen. After cooling, 10 ml of methanol are added and precipitation is allowed to take place. The solid obtained is filtered off and rinsed with methanol. Drying is carried out.
• Diethylamine (14.5 ml, 0.14 mol) and propargyl alcohol (6.81 ml, 0.1 17 mol) are dissolved in 100 ml of toluene.
• 34.5 g of manganese dioxide (activated, ⁇ 5 ⁇ ; 3.4 equiv.) are added portionwise while controlling the strong exotherm (temperature ⁇ 50°C) and the mixture is left stirring at 52°C for 20 hours.
• the reaction mixture is filtered.
• the yellow filtrate is poured into a reactor surmounted by a Dean and Stark apparatus.
• n-Octyl cyanoacetate 23 g, 0.1 17 mol
• catalyst 0.1 equiv., 0.667 ml of acetic acid and 1 .2 ml of N,N- diethylamine
• dichloromethane is added and washing is carried out once with a saturated sodium bicarbonate solution and then once with water.
• the organic phase is dried and then concentrated under vacuum.
• the brown red oil obtained is chromatographed on a silica column (gradient of eluents: heptane/AcOEt 90:10 to 80:20).
• Diethylamine (30 g, 0.41 mol) and propargyl alcohol (18.4 g, 0.328 mol) are dissolved in 250 ml of toluene. 72.6 g of manganese dioxide (activated, ⁇ 5 ⁇ ; 2.5 equiv.) are added portionwise while controlling the strong exotherm (temperature ⁇ 50°C) and the mixture is left stirring at 90°C for 5 hours.
• the reaction mixture is filtered.
• the yellow filtrate is poured into a reactor surmounted by a Dean and Stark apparatus.
• N,N-Dimethylacrolein (80.52 ml, 0.772 mol) is dissolved in 460 ml of toluene while bubbling with nitrogen and the catalyst, a mixture of acetic acid (8.85 ml, 0.2 equiv.) and of n-octylamine (3.83 ml, 0.03 equiv.), is added. The mixture is heated to reflux and methyl cyanoacetate (69.48 ml, 0.787 mol) is added dropwise over 45 minutes. The water is removed by azeotropic distillation. The reaction is halted after 2 hours 30 minutes. The solvent is evaporated under vacuum. 152 g of a light brown powder are obtained, which powder is crystallized from isopropanol to give 1 18.5 g (yield: 85%) of the derivative of Example 6 in the form of a pale yellow powder:
• N,N-Dimethylacrolein (37.4 ml, 0.374 mol) is dissolved in 500 ml of toluene while bubbling with nitrogen and the catalyst, a mixture of acetic acid (4.1 ml, 0.2 equiv.) and of n-octylamine (1 .8 ml, 0.03 equiv.), is added. The mixture is heated to reflux and n-octyl cyanoacetate (76 ml, 0.359 mol) is added dropwise over 25 minutes. The water is removed by azeotropic distillation. The reaction is halted after 2 hours. The solvent is evaporated under vacuum. 123 g of an orangey brown solid are obtained, which solid is recrystallized from isopropanol to give 1 18.5 g (yield: 85%) of the derivative of Example 7 in the form of pale yellow needles:
• a mixture of methyl cyanoacetate (1 .3 ml, 15 x 10 "3 mol), of solketal (1 .25 ml, 10 x 10 "3 mol) and of DMAP (2.7 mg, 0.03 equiv.) is heated at reflux with stirring for 30 hours in a reactor rendered inert with nitrogen. After cooling, the solvent is evaporated under vacuum and the brown oil obtained is chromatographed on a silica column (gradient of eluents: heptane/EtOAc from 90:10 to 80:20).
• Second stage Preparation of (2,2-dimethyl-1 ,3-dioxolan-4-yl)methyl (2E,4E)-2- cyano-5-(dimethylamino)penta-2,4-dienoate
• the preceding product 50 mg, 0.254 x 10 "3 mol
• the catalysts, n-octylamine (1 .3 ⁇ , 0.03 equiv.) and acetic acid (3 ⁇ , 0.2 equiv.) are brought to reflux in a reactor rendered inert with nitrogen.
• N,N-Dimethylacrolein (26 ⁇ , 0.25 x 10 "3 mol), dissolved in 0.8 ml of toluene, is added dropwise to the reaction mixture. Reflux is maintained for 36 hours while adding the same amounts of catalyst every 8 hours. After cooling, the solvent is evaporated under vacuum and the brown paste obtained is crystallized from 2 ml of isopropanol. 68 mg (yield: 97%) of (2,2-dimethyl-1 ,3-dioxolan-4-yl)methyl (2E,4E)-2-cyano-5-(dimethylamino)penta-2,4-dienoate are thus obtained in the form of a beige powder used as is in the following stage:
• Example 4 The derivative of Example 4 (15.5 g, 0.051 mol) is heated at 60°C for 2 hours with 100 ml of piperidine while bubbling with nitrogen. Heating is continued at 80°C for 6 hours. After cooling the reaction mixture, it is poured into 2 litres of water. The precipitate obtained is filtered off and is washed with 3 pistons of water. After drying, 12.57 g (yield: 75%) of the derivative of Example 9 are obtained in the form of a pale yellow powder:
• oil/water emulsions are prepared; the amounts are expressed percentages by weight, with respect to the total weight of each composition.
• the aqueous phase (Phase B) comprising all of its ingredients is heated to 80°C in a water bath.
• the fatty phase (Phase A) comprising all of its ingredients is heated to 80°C in a water bath.
• A is emulsified in B with stirring of rotor-stator type (device from Moritz).
• Phase C is incorporated and the mixture is allowed to return to ambient temperature with moderate stirring.
• the triethanolamine is introduced so as to adjust the pH to the value desired at the end of manufacture.
• the products are quantified by HPLC of the extracts.
• the degrees of loss are determined by comparison of the amounts of product present in the irradiated samples and in the non-irradiated controls prepared simultaneously and treated in the same way (means over 3 samples).
• the compounds of the invention (e), (f) and (g) respectively present in the formulations Ai to A 3 photostabilize the avobenzone better than the comparative compounds bi, b 2 , b 3 and b 4 present in the formulations Bi to B and do this in a significant way.
• the compounds of the invention (e), (f) and (g) respectively present in the formulations Ai to A 3 do not or virtually do not photodecompose in the presence of avobenzone, in contrast to the comparative compounds bi, b 2 , b 3 and b 4 .

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• 2011
  • 2011-03-07 BR BR112012022703-3A patent/BR112012022703B1/pt active IP Right Grant
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